Showing results (101-110 of 190) with videos related to

Sort By:
Pageof 19
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 5, 1998
Membrane-associated molecules guide limbic and nonlimbic thalamocortical projectionsF Mann, V Zhukareva, A Pimenta, et al.
The British Journal of Ophthalmology|October 25, 2014
A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod-cone dystrophy phenotype on the Arabian PeninsulaArif O Khan, Carsten Bergmann, Tobias Eisenberger, et al.
Journal of Pediatric Ophthalmology and Strabismus|July 18, 2014
Limited ocular motility in a child with 3q23 microdeletion ("blepharophimosis syndrome plus")Arif O Khan, Sandra Nagl, Carsten Bergmann, et al.
Ophthalmic Genetics|December 6, 2014
A distinct vitreo-retinal dystrophy with early-onset cataract from recessive KCNJ13 mutationsArif O Khan, Carsten Bergmann, Christine Neuhaus, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 30, 2017
[Genotype-Phenotype Correlations in Patients with CRB1 Mutations]C Papadopoulou Laiou, M N Preising, H J Bolz, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 10, 1998
Dual action of a ligand for Eph receptor tyrosine kinases on specific populations of axons during the development of cortical circuitsV Castellani, Y Yue, P P Gao, et al.
Development (Cambridge, England)|November 13, 1998
Semaphorins act as attractive and repulsive guidance signals during the development of cortical projectionsD Bagnard, M Lohrum, D Uziel, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 29, 1996
Virus-mediated gene transfer into hippocampal CA1 region restores long-term potentiation in brain-derived neurotrophic factor mutant miceM Korte, O Griesbeck, C Gravel, et al.
Pageof 19